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Peter G Gillespie

Showing results (41-50 of 50) with videos related to

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Neuron|August 17, 2005
Fast adaptation in vestibular hair cells requires myosin-1c activityEric A Stauffer, John D Scarborough, Moritoshi Hirono, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|October 6, 2006
The chloride intracellular channel protein CLIC5 is expressed at high levels in hair cell stereocilia and is essential for normal inner ear functionLeona H Gagnon, Chantal M Longo-Guess, Mark Berryman, et al.
Cell|February 21, 2002
A chemical-genetic strategy implicates myosin-1c in adaptation by hair cellsJeffrey R Holt, Susan K H Gillespie, D William Provance, et al.
Plos One|February 10, 2011
Na+/K+-ATPase α1 identified as an abundant protein in the blood-labyrinth barrier that plays an essential role in the barrier integrityYue Yang, Min Dai, Teresa M Wilson, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 10, 2004
Chemical-genetic inhibition of a sensitized mutant myosin Vb demonstrates a role in peripheral-pericentriolar membrane trafficD William Provance, Christopher R Gourley, Colleen M Silan, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|February 17, 2006
Physical and functional interaction between protocadherin 15 and myosin VIIa in mechanosensory hair cellsMathias Senften, Martin Schwander, Piotr Kazmierczak, et al.
Neuron|February 3, 2007
Hair bundles are specialized for ATP delivery via creatine kinaseJung-Bum Shin, Femke Streijger, Andy Beynon, et al.
Neuron|May 19, 2009
Harmonin mutations cause mechanotransduction defects in cochlear hair cellsNicolas Grillet, Wei Xiong, Anna Reynolds, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|July 28, 2010
The R109H variant of fascin-2, a developmentally regulated actin crosslinker in hair-cell stereocilia, underlies early-onset hearing loss of DBA/2J miceJung-Bum Shin, Chantal M Longo-Guess, Leona H Gagnon, et al.
American Journal of Human Genetics|January 25, 2011
Loss-of-function mutations of ILDR1 cause autosomal-recessive hearing impairment DFNB42Guntram Borck, Atteeq Ur Rehman, Kwanghyuk Lee, et al.
Pageof 5

Showing results (41-50 of 50) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 50 results.
Neuron|August 17, 2005
Fast adaptation in vestibular hair cells requires myosin-1c activityEric A Stauffer, John D Scarborough, Moritoshi Hirono, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|October 6, 2006
The chloride intracellular channel protein CLIC5 is expressed at high levels in hair cell stereocilia and is essential for normal inner ear functionLeona H Gagnon, Chantal M Longo-Guess, Mark Berryman, et al.
Cell|February 21, 2002
A chemical-genetic strategy implicates myosin-1c in adaptation by hair cellsJeffrey R Holt, Susan K H Gillespie, D William Provance, et al.
Plos One|February 10, 2011
Na+/K+-ATPase α1 identified as an abundant protein in the blood-labyrinth barrier that plays an essential role in the barrier integrityYue Yang, Min Dai, Teresa M Wilson, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 10, 2004
Chemical-genetic inhibition of a sensitized mutant myosin Vb demonstrates a role in peripheral-pericentriolar membrane trafficD William Provance, Christopher R Gourley, Colleen M Silan, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|February 17, 2006
Physical and functional interaction between protocadherin 15 and myosin VIIa in mechanosensory hair cellsMathias Senften, Martin Schwander, Piotr Kazmierczak, et al.
Neuron|February 3, 2007
Hair bundles are specialized for ATP delivery via creatine kinaseJung-Bum Shin, Femke Streijger, Andy Beynon, et al.
Neuron|May 19, 2009
Harmonin mutations cause mechanotransduction defects in cochlear hair cellsNicolas Grillet, Wei Xiong, Anna Reynolds, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|July 28, 2010
The R109H variant of fascin-2, a developmentally regulated actin crosslinker in hair-cell stereocilia, underlies early-onset hearing loss of DBA/2J miceJung-Bum Shin, Chantal M Longo-Guess, Leona H Gagnon, et al.
American Journal of Human Genetics|January 25, 2011
Loss-of-function mutations of ILDR1 cause autosomal-recessive hearing impairment DFNB42Guntram Borck, Atteeq Ur Rehman, Kwanghyuk Lee, et al.
Pageof 5